- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you ... will define, develop and lead global strategies to maximize global ...field as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceuticals (Lexington, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Affairs CMC where you ... strategies for assigned products. RA CMC member on the Global Regulatory CMC team. Serve as or... CMC team, you will report to a Senior Director and work with stakeholders across the business. **How… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning ... - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** ... vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory...members (Clinical, Global Patient Safety, Program Management, Global Regulatory , Regulatory Operations, Drug… more
- Takeda Pharmaceuticals (Lexington, MA)
- …the best of my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review out of our Lexington, MA or ... FDA law and regulations for development of marketing materials, including representation on global regulatory and labeling teams. + Provide leadership related to… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …is true to the best of my knowledge. **Job Description** **Objectives:** + The Associate Director , Global Scientific Communications, Mature Brands, is a ... Communications planning and execution for mature brands. + The Associate Director , Global Medical Communications...Material Review and Approval + Work with Legal and Regulatory colleagues to resolve questions and provide leadership in… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Evidence and Outcomes where you will lead ... the Global Evidence and Outcomes team, you will report to the Director , Global Evidence & Outcomes, Neuroscience. **How you will contribute:** + Collaborates… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director , Global Patient Safety Signal Management and Innovation ... processes and activities are compliant with EU regulations and EU regulatory authority and inspectors' expectations. You will develop, review, evaluate and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Global Medical Communications is a dynamic, strategic role ... + Manage Global Medical Communications planning and execution for GI + The Associate Director , Global Medical Communications leads and is accountable for… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Reporting into Global Medical Communications, the Associate Director , Global Medical ... + Develop and manage the annual congress strategic planning process for Global Medical Affairs (including forecasting +3 years) and ensuring proper linkage to… more
- Takeda Pharmaceuticals (Boston, MA)
- …and executes operational plans to enhance synergies and efficiencies across Global Publication Center of Excellence and Takeda-wide Publication Business Units and ... high quality publication types. + Leads vendor management activities with Global Publications and Procurement including communication of expectations and timelines,… more
- AbbVie (Cambridge, MA)
- …level will be determined by the qualifications listed below. Purpose: The Associate Scientific Director , Psychiatry Pipeline role provides medical and scientific ... other available training, to augment expertise in the therapeutic area. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the… more
- Sanofi Group (Cambridge, MA)
- …diseases. **Main Responsibilities:** The Early Pipeline Gastroenterology Associate Medical Director reports to the Global Medical Head of Immunology and ... **About the Job** We are an innovative global healthcare company, committed to transforming the lives...curate patient and scientific evidence and partner with commercial, regulatory , R&D, market access, and external affairs teams to… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Strategic Sourcing - R&D and Supply Chain/TOQ.** The ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...Associate Director Strategic Sourcing R&D and Supply… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , Clinical Quality Compliance **Location** : Cambridge, MA **About the ... role:** As the Associate Director , Clinical Quality Compliance, you will...include Global Development Office, Data Science Institute, Global Regulatory Affairs, Procurement, Legal. + Provide… more
- AbbVie (Cambridge, MA)
- …standards, including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational… more
- Merck (Boston, MA)
- …and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical Development organization ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… more
- Merck (Boston, MA)
- …the Research & Division organization of our company. **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early ... Description** The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- Bristol Myers Squibb (Devens, MA)
- …lives. Read more: careers.bms.com/working-with-us . **PURPOSE AND SCOPE OF POSITION:** The Associate Director , CTF Digital Plant IT Quality at Devens Cell ... including GAMP and ISO 9001. + Mastery of site and global SOPs, cGMPs, compliance requirements, regulatory guidelines (FDA, EU) and the technical acumen to work… more